Meet our “Allies For FPIES,” our partners for Global FPIES Day, 2020, here on this page and continued on this page. This year, we honor all of those who stand with our community to raise awareness, build community support, expand research, and improve quality of care for all those affected by FPIES.
“NORD and the NORD logo are registered trademarks
of the National Organization for Rare Disorders.
NORD is a registered 501(c)(3) charity.”
Alone we are rare. Together we are strong.®
NORD, a 501(c)(3) organization, is a patient advocacy organization dedicated to individuals with rare diseases and the organizations that serve them. NORD, along with its more than 300 patient organization members, is committed to the identification, treatment, and cure of rare disorders through programs of education, advocacy, research, and patient services. If you live with a rare disease, or love someone who does, NORD is here to help you. For more than 30 years, we have been providing services for patients and their families, rare disease patient organizations, medical professionals, and those seeking to develop new diagnostics and treatments. We are here to support every member of the rare disease community with programs and services focused on one ultimate goal: to improve the lives of individuals and families affected by rare diseases.
"An individual can make a change but a team can make a revolution" Amit Kalantri
Food Equality Initiative
"Unity is strength. . . where there is teamwork and collaboration, wonderful things can be achieved" -- Mattie Stepanek
"Lighting the path for others illuminates our own journey."
"Alone we can do so little, together we can do so much" -- Hellen Keller
Becoming an Ally for FPIES
Organizations that The FPIES Foundation decides to partner with are carefully reviewed for credibility and reliability of resources before The FPIES Foundation initiates projects relating to partnerships. Partnerships are based upon the credibility of the organizations in question and the applicability of resources such organizations may offer in regards to benefiting the community of families and medical providers who support individuals diagnosed with FPIES.
The FPIES Foundation is an Incorporated 501(c)3 Non-profit foundation dedicated to overcoming the challenges of FPIES by offering tools for education, support, and advocacy to empower families and the medical community.
Page published: September 16, 2020. Last Updated: October 8, 2020. Copyright ©2020 The FPIES Foundation